Synopsis
Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
0
API
0
FDF
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
EDQM
0
USP
0
JP
0
Others
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
1. 7440-63-3
2. Xe
3. Xenon Atom
4. Chebi:49957
5. Xenon (jan)
6. 3h3u766w84
7. 20222-53-1
8. Xenon [jan]
9. Einecs 231-172-7
10. Un2036
11. Un2591
12. Xenon Dihydride
13. Xenon Hydride
14. Unii-3h3u766w84
15. Xenon, Compressed
16. Xenopure (tn)
17. Xenon(0)
18. Xenon [vandf]
19. Xenon 99+%
20. Xenon [who-dd]
21. Xenon [mart.]
22. Xenon [mi]
23. [xe]
24. 54xe
25. Xenon,isotope Of Mass 123
26. Chembl1236802
27. Dtxsid5064700
28. Chebi:49956
29. Xenon, >=99.995%
30. Mfcd00036280
31. Akos025310455
32. Db13453
33. Xenon, 99.99%, Messer(r) Cangas
34. Q1106
35. D01901
36. Xenon, Refrigerated Liquid (cryogenic Liquids)
37. Xenon, Compressed [un2036] [nonflammable Gas]
38. Xenon, Refrigerated Liquid (cryogenic Liquids) [un2591] [nonflammable Gas]
| Molecular Weight | 131.29 g/mol |
|---|---|
| Molecular Formula | Xe |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 0 |
| Exact Mass | 131.90415508 g/mol |
| Monoisotopic Mass | 131.90415508 g/mol |
| Topological Polar Surface Area | 0 Ų |
| Heavy Atom Count | 1 |
| Formal Charge | 0 |
| Complexity | 0 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Anesthetics, Inhalation
Gases or volatile liquids that vary in the rate at which they induce anesthesia; potency; the degree of circulation, respiratory, or neuromuscular depression they produce; and analgesic effects. Inhalation anesthetics have advantages over intravenous agents in that the depth of anesthesia can be changed rapidly by altering the inhaled concentration. Because of their rapid elimination, any postoperative respiratory depression is of relatively short duration. (From AMA Drug Evaluations Annual, 1994, p173) (See all compounds classified as Anesthetics, Inhalation.)
N - Nervous system
N01 - Anesthetics
N01A - Anesthetics, general
N01AX - Other general anesthetics
N01AX15 - Xenon
API SUPPLIERS
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USDMF
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API Imports and Exports
| Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
|---|
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ABOUT THIS PAGE
A Xenon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Xenon, including repackagers and relabelers. The FDA regulates Xenon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Xenon API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Xenon supplier is an individual or a company that provides Xenon active pharmaceutical ingredient (API) or Xenon finished formulations upon request. The Xenon suppliers may include Xenon API manufacturers, exporters, distributors and traders.
click here to find a list of Xenon suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Xenon DMF (Drug Master File) is a document detailing the whole manufacturing process of Xenon active pharmaceutical ingredient (API) in detail. Different forms of Xenon DMFs exist exist since differing nations have different regulations, such as Xenon USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Xenon DMF submitted to regulatory agencies in the US is known as a USDMF. Xenon USDMF includes data on Xenon's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Xenon USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Xenon suppliers with USDMF on PharmaCompass.
Xenon Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Xenon GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Xenon GMP manufacturer or Xenon GMP API supplier for your needs.
A Xenon CoA (Certificate of Analysis) is a formal document that attests to Xenon's compliance with Xenon specifications and serves as a tool for batch-level quality control.
Xenon CoA mostly includes findings from lab analyses of a specific batch. For each Xenon CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Xenon may be tested according to a variety of international standards, such as European Pharmacopoeia (Xenon EP), Xenon JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Xenon USP).
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